| Tag | Content |
|---|
EnhancerAtlas ID | HS151-04305 |
Organism | Homo sapiens |
Tissue/cell | OCI-LY1 |
Coordinate | chr16:3637390-3638460 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr16:3637638-3637649 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr16:3637638-3637649 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_60927 | chr16:3624790-3638705 | DHL6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGAGGCTGAG GCAGGAGAAT CCCTTGAACC CGAGAGGTGG AGGTTGCAGT GAGCCGAGAT 60
AGCCCCACTG CACTCCAGCC TGGTGACACA TTGGAAACAG TCAGACTTTG GTTCTTCTGC 120
CTTTTATGAC CATGGAGCCC TTTGAGCCCC CGATGAAAGC GGCAGGCTCT GTCTCCTGAG 180
AAAAGCACGA TTCTTCCTGT GGCCGCAGCG TCGTCCTGAA GCCCACCTCA GATCTGCTGT 240
GCAGCCTCCT GCAGCTGTTC TCACAGCACT GCCTGGGAAC TGGTTAGAAA TGCAAATTCT 300
TAGTCACCCT CCCGAAGCAA GGCTCTGGGG CAGGCTGGGC CACGGGCGTG CTATAAGAAG 360
CTCTCCAGGT GTTTCTGAAG CCCCTGAGGG CCGAGGACAC TATCAGTGGC CTCATTCATC 420
TGGATTTTGG GAGGAAATGG GCCCCCAGGC CGCAGGCAGG TGCTCACTCA CAGCCTGGCC 480
TTTCTCCCAG TCATGCTCAG CCCAGCCCGG CCTGTCCTTG CCCTCCCCGG AGGTGCCTGG 540
ATGGGAGCAG CAGCACCGAG GGGGCCGACA CCTGGGGCTC TGACTCTCCC CGGGGACTGA 600
AATGAGCAGG GAGGTGGCAT CCCTGCACCT GGGAGGACCA GGAAGAACAG GCCTAACAGC 660
CTCTCACACT TGTCCCACCT GATTCTTTTT TTAATTGAGG TGAAATTCAC ATAAAAAAAT 720
CGTAAAGGGA ATAATTCAGT GGCATTAAGT ATTCACAATG TTGTACAACC ATCACCTCTA 780
TCTATTTGCA AAACATTTTC ACCACCCCAA AAGGACACCC TGTATCCCAT AAGCAGTCAC 840
TCCCCATTCC CCCTCCCTCC AACCCAGGCC AACCACTAAC CTGCATTTTC TCTGGATTTG 900
CCTATTCTAG ACATTTCATA TCCATGAGTG CAGACAGTAC ATGACCTTCT ATGTCTGGCT 960
TCTCTCACCC GGCAGCATGT TTTCTGGGTC GTCCACGCGG TAGCGTGTGG CAGTGCCTCA 1020
CTCCTCTTTG TGGCTGAACA CTATTCCATT TTCTAGTGGT CTAGATGGAC 1070
|
